Article
Abnormal spermatozoa in the ejaculate: abortive apoptosis and faulty nuclear remodelling during spermatogenesis

https://doi.org/10.1016/S1472-6483(10)61886-XGet rights and content

Abstract

The mechanisms responsible for producing abnormal spermatozoa in the ejaculate are relatively unknown. Numerous studies have now shown the presence of nuclear DNA strand breaks in human ejaculated spermatozoa and the abnormal persistence of apoptotic marker proteins. The reason why human spermatozoa, in particular from men with abnormal semen parameters, possess these abnormalities is still not clear. Two processes that have been linked to the presence of nuclear DNA strand breaks in spermatozoa are anomalies in apoptosis during spermatogenesis or problems in the replacement of histones with protamines during spermiogenesis. Understanding the mechanisms responsible for producing abnormal spermatozoa in the human will improve knowledge about certain causes of male infertility.

Section snippets

Dr Denny Sakkas obtained his PhD at Monash University, Australia. Since then he has headed research groups and directed In Vitro Fertilization Laboratories at the University of Geneva, and Birmingham, UK, and currently in the Department of Obstetrics at Yale University. His research interests include: (i) understanding the role of apoptosis and presence of nuclear DNA damage in the spermatozoa of men with poor semen parameters; (ii) the consequences of using abnormal spermatozoa to fertilize

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    Dr Denny Sakkas obtained his PhD at Monash University, Australia. Since then he has headed research groups and directed In Vitro Fertilization Laboratories at the University of Geneva, and Birmingham, UK, and currently in the Department of Obstetrics at Yale University. His research interests include: (i) understanding the role of apoptosis and presence of nuclear DNA damage in the spermatozoa of men with poor semen parameters; (ii) the consequences of using abnormal spermatozoa to fertilize eggs on the developing embryo and ensuing fetus; (iii) the role of glucose during gamete fusion; and (iv) examining for markers of preimplantation embryos, which help to predict subsequent viability.

    Paper based on contribution presented at the ‘TWIN-Meeting Alpha-Andrology 2003’ in Antwerp, Belgium, September 2003.

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